Relevant bibliographies by topics / Health researchers

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Health researchers'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Health researchers"

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Ramsay, Sarah. "African health researchers unite." Lancet 360, no. 9346 (November 2002): 1665–66. http://dx.doi.org/10.1016/s0140-6736(02)11654-0.

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Lewis, David C., and Eric M. Klinenberg. "Researchers and Health Care Reform." Alcoholism: Clinical and Experimental Research 18, no. 4 (August 1994): 771–73. http://dx.doi.org/10.1111/j.1530-0277.1994.tb00038.x.

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Thomas, Sandra P. "Barefoot Researchers in Mental Health?" Issues in Mental Health Nursing 37, no. 5 (May 3, 2016): 283–84. http://dx.doi.org/10.3109/01612840.2016.1165056.

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Plegue, Melissa. "An Introduction toSTATAfor Health Researchers." International Statistical Review 83, no. 3 (November 17, 2015): 511–12. http://dx.doi.org/10.1111/insr.12142.

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Guerriero, Iara Coelho Zito, and Sueli Gandolfi Dallari. "The need for adequate ethical guidelines for qualitative health research." Ciência & Saúde Coletiva 13, no. 2 (April 2008): 303–11. http://dx.doi.org/10.1590/s1413-81232008000200002.

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This paper discusses adequacy as to the application of Brazilian guidelines, Resolution 196/96¹ and complementaries to qualitative health researches, considering that these are based on non-positivistic paradigms. Frequently, decisions about the research are made together with the studied community. There is a concern with justice and social change. And, since subjectivity can be considered their privileged instrument, such researchers seek a balance between objectivity and subjectivity, discussing how to overcome the researcher's view. We have studied the application and the concept of research found in international and in the Brazilian guidelines. We have noticed that they adopt a positivist conception of research, which establishes 1) the hypothesis test, 2) that all procedures are previously defined by the researcher; 3) neutrality of the researcher and of the knowledge produced. We will present some characteristics of qualitative research; the ethical implications in the way as qualitative research is conceived in non-positivist paradigms and a brief history of these guidelines. Our conclusion: it is inadequate to analyze qualitative researches using these documents, and we suggest the design of specific guidelines for them.
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Gluud, Christian. "Danish health researchers kept in suspense." Lancet 346, no. 8976 (September 1995): 691. http://dx.doi.org/10.1016/s0140-6736(95)92292-x.

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Doupe, Patrick, James Faghmous, and Sanjay Basu. "Machine Learning for Health Services Researchers." Value in Health 22, no. 7 (July 2019): 808–15. http://dx.doi.org/10.1016/j.jval.2019.02.012.

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Lough, Shannon. "Health researchers highlighted in online project." Canadian Medical Association Journal 187, no. 10 (May 25, 2015): E292. http://dx.doi.org/10.1503/cmaj.109-5074.

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O'Neill, Gareth, and Mathias Schroijen. "Early-career researchers and mental health." Impact 2018, no. 10 (December 21, 2018): 4–5. http://dx.doi.org/10.21820/23987073.2018.10.4.

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O'Neill, Gareth, and Mathias Schroijen. "Early-career researchers and mental health." Impact 2018, no. 12 (December 31, 2018): 44–45. http://dx.doi.org/10.21820/23987073.2018.12.44.

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Dissertations / Theses on the topic "Health researchers"

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Malins, Gillian Leigh. "Mental health consumers' experiences of becoming evaluation researchers." Access electronically, 2005. http://www.library.uow.edu.au/adt-NWU/public/adt-NWU20060307.113753/index.html.

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Williams, Stacey L. "LGBT Health Disparities: Rallying Stigma and Intergroup Relations Researchers." Digital Commons @ East Tennessee State University, 2014. https://dc.etsu.edu/etsu-works/8090.

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Williams, Stacey L. "Mobilizing Intergroup Relations and Stigma Researchers Around LGBT Health Disparities." Digital Commons @ East Tennessee State University, 2017. https://dc.etsu.edu/etsu-works/8053.

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Sofia, Gustina, and n/a. "Information needs of health researchers at the National Institute of Health Research and Development, Ministry of Health, Indonesia." University of Canberra. Information, Language & Culture, 1992. http://erl.canberra.edu.au./public/adt-AUC20061109.083237.

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The present study attempted to investigate the information needs/information seeking behaviour of health researchers at the National Institute of Health Research and Development, Ministry of Health, Indonesia. Its objective was to identify the relationship between information needs/information seeking behaviour and the characteristics of those health professionals. Those characteristics include institution to which health professionals belonged, institution geographic location, level of appointment, level of education, and work experience. Research was carried out through survey by using a questionnaire. This survey obtained a response rate of 92 percent from a sample of 131 health professionals. Their information needs/information seeking behaviour were correlated with their characteristics to determine relationships, and the Statistical Package for the Social Sciences (SPSS) was used to analyse the data. Frequency distribution, chi-square analysis, and descriptive analysis were used to obtain the results. The study found that the health information available did not match the health professionals' needs and that there was strong demand by these personnel for automated information services. It also found that total hours reading per week was significantly related to level of appointment, level of education, and work experience at other institutions. The perceived usefulness of journals as information sources was significantly related to institution, geographic location, level of appointment, level of education and work experience at other institutions. Government publications and statistical data as a source of information were found to be related significantly to institution and geographic location. There was also a relationship between the perceived value of reference books and work experience at the current institution. The usefulness of library catalogues as a guide to information was found to be related significantly to institution and geographic location, as was the usefulness of abstracting and indexing services to level of education. Frequency of visiting libraries was significantly related to institution, geographic location and level of appointment. The membership of professional organizations and obtaining useful information from friends, colleagues or personal contact were found to be significantly related to level of education. The study concludes with recommendations and suggestions for further research.
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Hancock, Beverley. "The development of career researchers from the NHS primary health care professional workforce." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440999.

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Davies, Alun Iwan. "Expectations, experiences and impact of engagement between health researchers and schools in Kenya." Thesis, Open University, 2017. http://oro.open.ac.uk/52220/.

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Community engagement is increasingly recognized as essential for the ethical conduct of health research, particularly in international settings where wealth, educational and cultural differences between host communities and researchers are often stark. Engagement approaches are diverse, addressing a wide range of goals. The School Engagement Programme (SEP) forms part of a wider platform of community engagement activities at the KEMRI-Wellcome Trust Research Programme (KWTRP) in Kilifi, Kenya. Key SEP goals include raising mutual understanding between researchers and community members, nurturing secondary school students’ interest in science, and raising educational aspirations. In this thesis, I address the paucity of careful evaluations of community engagement in low and middle-income countries (LMICs), and of school engagement specifically. I consider the potential contribution of school engagement to the ethical goals of research, and contribute to the identification of key elements to use in the evaluation of school engagement programmes in the region. Drawing on a novel combination of methods including participatory video, baseline and post-intervention surveys, interviews and group discussions I found that the SEP benefitted students through nurturing an interest in science and promoting confidence in speaking to researchers, laying a foundation for future interactions. Researchers benefitted through strengthened ties with the community which gave them a better understanding of the context of their work and more of a sense of being part of the community. There were also unintended outcomes and mismatches between programme goals and community expectations however, which highlight the need for broad inclusion in planning and implementing school engagement programmes, and the monitoring of perverse outcomes. The thesis draws from the SEP evaluation findings to synthesise a theory of change and a framework to guide the evaluation of school engagement programmes.
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King-Moore, Dorothy. "Researchers', Stakeholders', and Investors' Perceptions of U.S. Stem Cell Research Policy." ScholarWorks, 2017. https://scholarworks.waldenu.edu/dissertations/3947.

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Federal support and funding for human embryonic stem cell (hESC) research in the United States lags behind stem cell programs in many countries because of the divisive debate over hESC research and the continually evolving federal policies that have hindered research efforts. The purpose of this phenomenological study was to explore the perceptions of stem cell researchers, stakeholders, and investors in the United States about the effects of the current federal stem cell policy on stem cell research in the United States, the moral disagreement with stem cell research, and their recommendations to improve stem cell research policy in the United States. Rogers's diffusion of innovation theory and Kingdon's agenda-setting theory served as the theoretical frameworks for this study. Data were collected through telephonic semistructured interviews with a snowball sample of 21 participants. Data were analyzed using Attride-Stirling's 6 steps of thematic coding. Findings indicated the need to educate laypersons and legislators, involve the public in the stem cell research policy debate, increase federal funding, and exclude religious considerations from political discussions. The implications for positive social change are directed at stem cell policymakers to focus attention and resources on creating a cohesive federal hESC funding policy to ensure that stem cell research improves in the United States with the goal of developing treatments for conditions that are currently untreatable.
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Baker, Erin R. "Attitudes and Practices of NIH-funded Researchers Toward Reporting Individual Test Results to Research Subjects." University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1147100909.

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Singler, Mary E. "Perspectives on the meaning and significance of imagery| A survey of clinicians, educators, and researchers." Thesis, Saybrook University, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3683095.

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The purpose of this qualitative descriptive research study was to delineate the perspectives held by medical experts on the meaning and significance of imagery. Thirteen doctorate-prepared experts, including clinicians, educators, and researchers, were surveyed via email and asked basic demographic information and their responses to five open-ended questions. The questions were designed to elicit the experts' perceptions regarding their definition of imagery; the significance of imagery to health; the role of imagery in the experts' professional practices; and the potential relationships that exist between imagery and psychoneuroimmunology (PNI), and imagery and the learning domains.

Literature from systems theory provided the conceptual framework for this study and a philosophical approach influenced the research design. The study utilized a manual content analysis to identify themes that best described the experts' perspectives. The following three themes emerged: (a) Imagery is a complex construct comprised of both structural and process components which are interconnected via a complex communication system, which responds, directs, and transmits the flow of information within the individual and also between the individual and the environment. (b) The structural component of imagery is multisensorial, multifaceted, and it influences and is influenced by the learning and health domains resulting in the potential for both positive and adverse effects on health. (c) When imagery's process component is used and directed in a goal-oriented, purposeful, intention-driven way, desired outcomes can be achieved in the psychophysiological domains of health.

The purpose of seeking the experts' perspectives on the meaning and significance of imagery was to gain a better understanding of imagery's role in influencing health. Expanded perspectives were sought because health-risk behaviors are contributing to the rising prevalence of chronic disease in America, which in turn, supports a costly medical model of disease-management rather than one that promotes health. It was concluded that maximizing positive imagery could not only be a potential mechanism for addressing the issues related to chronic disease, but also an effective way to improve the health of the nation.

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Berrisford, Isabelle C. "Dual Agency of Physician-Researchers: The Role of Equipoise in RCTs in Preserving the Integrity of the Physician-Researcher Role During Public Health Crises." The Ohio State University, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1619164005499914.

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Books on the topic "Health researchers"

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An introduction to Stata for health researchers. 2nd ed. College Station, Texas: Stata, 2008.

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Morten, Frydenberg, ed. An introduction to Stata for health researchers. 3rd ed. College Station, Tex: Stata Press, 2010.

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Juul, Svend. An introduction to Stata for health researchers. 2nd ed. College Station, Texas: Stata, 2008.

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Gafour, M. J. One thousand health care Internet sites for health professionals & researchers. Reading: M. Osborne, 1990.

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Spasoff, R. A. Health data for public health: A manual for public health planners and researchers. Ottawa: University of Ottawa, 1993.

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The health project book: A handbook for new researchers in the field of health. London: Routledge, 2001.

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Moral entanglements: The ancillary-care obligations of medical researchers. Oxford: Oxford University Press, 2012.

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Iles, Valerie. Organisational change: A review for health care managers, professionals and researchers. London: NCCSDO, 2001.

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Anthony, Denis. Understanding advanced statistics: A guide for nurses and health care researchers. Edinburgh: Churchill Livingstone, 1999.

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Katz, Mitchell H. Multivariable Analysis: A Practical Guide for Clinicians and Public Health Researchers. 3rd ed. Leiden: Cambridge University Press, 2011.

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Book chapters on the topic "Health researchers"

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Roberts, Chris, and Stephen Loftus. "The Development of Healthcare Researchers." In Educating Health Professionals, 159–72. Rotterdam: SensePublishers, 2013. http://dx.doi.org/10.1007/978-94-6209-353-9_14.

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Crasto, Chiquito J. "Bioinformatics for Biological Researchers—Using Online Modalities." In Health Informatics, 147–65. London: Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4078-8_11.

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Martínez-Nicolás, Israel, and Jorge García-Girón. "“No Future for You”: Economic and Mental Health Risks in Young Spanish Researchers." In Researchers at Risk, 103–14. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-53857-6_7.

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Delman, Jonathan, and Alisa Lincoln. "Service Users as Paid Researchers." In Handbook of Service User Involvement in Mental Health Research, 139–51. Chichester, UK: John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9780470743157.ch10.

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Hao, Tianyong, Alex Rusanov, and Chunhua Weng. "Extracting and Normalizing Temporal Expressions in Clinical Data Requests from Researchers." In Smart Health, 41–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39844-5_7.

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Davies, Allyson Ross. "Health Care Researchers’ Needs for Computer-based Patient Records." In Aspects of the Computer-based Patient Record, 46–56. New York, NY: Springer New York, 1992. http://dx.doi.org/10.1007/978-1-4757-3873-5_7.

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Schaefer-McDaniel, Nicole, and Allison N. Scott. "Benefits and Challenges of Transdisciplinary Research for Urban Health Researchers." In Converging Disciplines, 13–22. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6330-7_2.

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Sabel, Clive E., Prince M. Amegbor, Zhaoxi Zhang, Tzu-Hsin Karen Chen, Maria B. Poulsen, Ole Hertel, Torben Sigsgaard, Henriette T. Horsdal, Carsten B. Pedersen, and Jibran Khan. "Urban Health and Wellbeing." In Urban Informatics, 259–80. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-8983-6_17.

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AbstractThis chapter explores how the Internet of Things and the utilization of cutting-edge information technology are shaping global research and discourse on the health and wellbeing of urban populations. The chapter begins with a review of smart cities and health and then delves into the types of data available to researchers. The chapter then discusses innovative methods and techniques, such as machine learning, personalized sensing, and tracking, that researchers use to examine the health and wellbeing of urban populations. The applications of these data, methods, and techniques are then illustrated taking examples from BERTHA (Big Data Centre for Environment and Health) based at Aarhus University, Denmark. The chapter concludes with a discussion on issues of ethics, privacy, and confidentiality surrounding the use of sensitive and personalized data and tracking or sensing individuals across time and urban space.
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Kemper, H. C. G. "Genesis of the Study and Acknowledgements to Subjects, Authors, Researchers and Sponsors." In Amsterdam Growth and Health Longitudinal Study (AGAHLS), 1–4. Basel: KARGER, 2003. http://dx.doi.org/10.1159/000076191.

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Maddalena, Victor. "Evidence-Based Decision-Making 8: Health Policy, a Primer for Researchers." In Methods in Molecular Biology, 501–17. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2428-8_30.

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Conference papers on the topic "Health researchers"

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"Adoption of Health Information Systems in Sri Lanka." In Universal Researchers. Universal Researchers, 2015. http://dx.doi.org/10.17758/ur.u0315204.

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Kalimeri, Kyriaki. "Session details: Young Researchers Forum." In DPH2019: 9th International Digital Public Health Conference (2019). New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3372929.

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Windle, Richard, Nilgün Göktepe, Heather Wharrad, Michael Taylor, Amanda Hill, Ayişe Karadağ, Zuhal Zeybekoğlu, and Seda Akgül. "TRAINING HEALTH RESEARCHERS BY EXPERIENCE-SHARING, HARNESSING ONLINE LEARNING DEVELOPMENT." In 13th International Conference on Education and New Learning Technologies. IATED, 2021. http://dx.doi.org/10.21125/edulearn.2021.2482.

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Marada, Jan, and Eva Hoke. "HEALTH RISKS OF BUYING IMPORTED TOYS." In 16th International Bata Conference for Ph.D. Students and Young Researchers. Tomas Bata University in Zlín, 2020. http://dx.doi.org/10.7441/dokbat.2020.29.

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Virk, Amrit, Tim Ensor, William Bolton, David Jayne, and Rebecca King. "O15 Building sustainable partnerships with local researchers for qualitative health systems research." In Crafting the future of qualitative health research in a changing world abstracts. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjopen-2019-qhrn.15.

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Moss, Laura, Martin Shaw, Ian Piper, Christopher Hawthorne, and John Kinsella. "Sharing of Big Data in Healthcare: Public Opinion, Trust, and Privacy Considerations for Health Informatics Researchers." In 10th International Conference on Health Informatics. SCITEPRESS - Science and Technology Publications, 2017. http://dx.doi.org/10.5220/0006251504630468.

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Wilson, Danyell S., Joel Aliancy, Kenneth Shain, Nicholas Eustace,, Eric Haura, Beulah Joseph, Keiran Smalley, et al. "Abstract B29: Training cancer researchers that are community advocates." In Abstracts: AACR International Conference on the Science of Cancer Health Disparities‐‐ Sep 30-Oct 3, 2010; Miami, FL. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1055-9965.disp-10-b29.

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Fleisher, Linda, and Carrie Norbeck. "Abstract C04: Cancer Disparities Research Network: Facilitating health disparities research and building the next generation of health disparities researchers." In Abstracts: Eighth AACR Conference on The Science of Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; November 13-16, 2015; Atlanta, Georgia. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7755.disp15-c04.

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Zimmermann, C., L. Föttinger, and C. Vajda. "Ressourcen für einen guten Karrierestart – Workshop der ÖGPH-Kompetenzgruppe Early Career Public Health Researchers." In 23. wissenschaftliche Tagung der Österreichischen Gesellschaft für Public Health (ÖGPH). © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1709060.

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Alekseev, Boris E., Alyona I. Skorobogatova, Dmitrii A. Egorov, and Aleksei A. Anisimov. "Baroreflex Function Analysis for Assessing the Cardiovascular System's Health." In 2021 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (ElConRus). IEEE, 2021. http://dx.doi.org/10.1109/elconrus51938.2021.9396321.

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Reports on the topic "Health researchers"

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Wendland, Lori, Harold Balbach, Mary Brown, Joan D. Berish, Ramon Littell, and Melissa Clark. Handbook on Gopher Tortoise (Gopherus polyphemus): Health Evaluation Procedures for Use by Land Managers and Researchers. Fort Belvoir, VA: Defense Technical Information Center, January 2009. http://dx.doi.org/10.21236/ada501295.

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Reichenbach, Laura, Carolyn Rodehau, Emily Peca, and John Stanback. Implementation science approaches to family planning and reproductive health: Experiential learning and sharing for implementers, policy-makers, researchers, and advocates. Population Council, 2016. http://dx.doi.org/10.31899/rh8.1056.

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Mahling, Alexa, Michelle LeBlanc, and Paul A. Peters. Report: Rural Resilience and Community Connections in Health: Outcomes of a Community Workshop. Spatial Determinants of Health Lab, Carleton University, December 2020. http://dx.doi.org/10.22215/sdhlab/2020.1.

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Canadians living in rural communities are diverse, with individual communities defined by unique strengths and challenges that impact their health needs. Understanding rural health needs is a complex undertaking, with many challenges pertaining to engagement, research, and policy development. In order to address these challenges, it is imperative to understand the unique characteristics of rural communities as well as to ensure that the voices of rural and remote communities are prioritized in the development and implementation of rural health research programs and policy. Effective community engagement is essential in order to establish rural-normative programs and policies to improve the health of individuals living in rural, remote, and northern communities. This report was informed by a community engagement workshop held in Golden Lake, Ontario in October 2019. Workshop attendees were comprised of residents from communities within the Madawaska Valley, community health care professionals, students and researchers from Carleton University in Ottawa, Ontario, and international researchers from Australia, Sweden, and Austria. The themes identified throughout the workshop included community strengths and initiatives that are working well, challenges and concerns faced by the community in the context of health, and suggestions to build on strengths and address challenges to improve the health of residents in the Madawaska Valley.
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Shannon, Caitlin S., and Beverly Winikoff. Misoprostol: An emerging technology for women's health—Report of a seminar. Population Council, 2004. http://dx.doi.org/10.31899/rh17.1002.

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On May 7–8, 2001, the Population Council and the Center for Reproductive Health Research & Policy of the University of California, San Francisco, convened a technical seminar in New York City on the use of misoprostol for women’s health indications. The seminar was designed to provide a forum for researchers, providers, women’s health advocates, and educators to exchange information with the goal of advancing the potential of misoprostol to improve women’s health. Participants discussed the state of the art in research, examined current clinical use of misoprostol, and created strategies for the future. The first day focused on scientific and clinical aspects of misoprostol use. The second day’s discussion centered on the future of misoprostol for women’s health, including identifying priorities for research and the role of provider groups and women’s health and advocacy organizations in helping to ensure misoprostol’s continued, appropriate use. At the end of each session, the group had an opportunity to share ideas and discuss unanswered questions. This report covers the key issues raised by each speaker and highlights general areas of discussion among participants.
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Bayley, Stephen, Darge Wole, Louise Yorke, Paul Ramchandani, and Pauline Rose. Researching Socio-Emotional Learning, Mental Health and Wellbeing: Methodological Issues in Low-Income Contexts. Research on Improving Systems of Education (RISE), April 2021. http://dx.doi.org/10.35489/bsg-rise-wp_2021/068.

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This paper explores methodological issues relating to research on children’s socio-emotional learning (SEL), mental health and wellbeing in low- and lower-middle-income countries. In particular, it examines the key considerations and challenges that researchers may face and provides practical guidance for generating reliable and valid data on SEL, mental health and wellbeing in diverse settings and different cultural contexts. In so doing, the paper draws on the experience of recent research undertaken in Ethiopia to illustrate some of the issues and how they were addressed. The present study extends earlier 2018-2019 RISE Ethiopia research, expanding its scope to consider further aspects of SEL, mental health and wellbeing in the particular context of COVID-19. In particular, the research highlights that the pandemic has brought to the fore the importance of assessing learning, and learning loss, beyond academic learning alone.
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Mirel, Lisa, Cindy Zhang, Christine Cox, Ye Yeats, Félix Suad El Burai, and Golden Cordell. Comparative analysis of the National Health and Nutrition Examination Survey public-use and restricted-use linked mortality files. Centers for Disease Control and Prevention (U.S.), May 2021. http://dx.doi.org/10.15620/cdc:104744.

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"Objectives—Linking national survey data with administrative data sources enables researchers to conduct analyses that would not be possible with each data source alone. Recently, the Data Linkage Program at the National Center for Health Statistics (NCHS) released updated Linked Mortality Files, including the National Health and Nutrition Examination Survey data linked to the National Death Index mortality files. Two versions of the files were released: restricted-use files available through NCHS and Federal Statistical Research Data Centers and public-use files. To reduce the reidentification risk, statistical disclosure limitation methods were applied to the public-use files before they were released. This included limiting the amount of mortality information available and perturbing cause of death and follow-up time for select records. Methods—To assess the comparability of the restricted-use and public-use files, relative hazard ratios for all-cause and cause-specific mortality using Cox proportional hazards models were estimated and compared. Results—The comparative analysis found that the two data files yield similar descriptive and model results. Suggested citation: Mirel LB, Zhang C, Cox CS, Ye Y, El Burai Félix S, Golden C. Comparative analysis of the National Health and Nutrition Examination Survey public-use and restricted-use linked mortality files. National Health Statistics Reports; no 155. Hyattsville, MD: National Center for Health Statistics. 2021. DOI: https://doi.org/10.15620/cdc:104744. CS323656 nhsr155-508.pdf"
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Arnold, Zachary, Rebecca Gelles, and Ilya Rahkovsky. Identifying AI-Related Companies: A Conceptual Outline and Proof of Concept. Center for Security and Emerging Technology, July 2020. http://dx.doi.org/10.51593/20200018.

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Artificial intelligence is of increasing interest to the private sector, but what exactly constitutes an “AI company?” This data brief offers a flexible, data-driven framework for identifying the companies most relevant in this field at the moment, providing policymakers and researchers with a tool for mapping technology transfer risks and gauging the overall health of America’s AI sector.
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8

Hilbrecht, Margo, David Baxter, Alexander V. Graham, and Maha Sohail. Research Expertise and the Framework of Harms: Social Network Analysis, Phase One. GREO, December 2020. http://dx.doi.org/10.33684/2020.006.

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In 2019, the Gambling Commission announced a National Strategy to Reduce Gambling Harms. Underlying the strategy is the Framework of Harms, outlined in Measuring gambling-related harms: A framework for action. "The Framework" adopts a public health approach to address gambling-related harm in Great Britain across multiple levels of measurement. It comprises three primary factors and nine related subfactors. To advance the National Strategy, all componentsneed to be supported by a strong evidence base. This report examines existing research expertise relevant to the Framework amongacademics based in the UK. The aim is to understand the extent to which the Framework factors and subfactors have been studied in order to identify gaps in expertise and provide evidence for decision making thatisrelevant to gambling harms research priorities. A social network analysis identified coauthor networks and alignment of research output with the Framework. The search strategy was limited to peer-reviewed items and covered the 12-year period from 2008 to 2019. Articles were selected using a Web of Science search. Of the 1417 records identified in the search, the dataset was refined to include only those articles that could be assigned to at least one Framework factor (n = 279). The primary factors and subfactors are: Resources:Work and Employment, Money and Debt, Crime;Relationships:Partners, Families and Friends, Community; and Health:Physical Health, Psychological Distress, and Mental Health. We used Gephi software to create visualisations reflecting degree centrality (number of coauthor networks) so that each factor and subfactor could be assessed for the density of research expertise and patterns of collaboration among coauthors. The findings show considerable variation by framework factor in the number of authors and collaborations, suggesting a need to develop additional research capacity to address under-researched areas. The Health factor subcategory of Mental Health comprised almost three-quarters of all citations, with the Resources factor subcategory of Money and Debt a distant second at 12% of all articles. The Relationships factor, comprised of two subfactors, accounted for less than 10%of total articles. Network density varied too. Although there were few collaborative networks in subfactors such as Community or Work and Employment, all Health subfactors showed strong levels of collaboration. Further, some subfactors with a limited number of researchers such as Partners, Families, and Friends and Money and debt had several active collaborations. Some researchers’ had publications that spanned multiple Framework factors. These multiple-factor researchers usually had a wide range of coauthors when compared to those who specialised (with the exception of Mental Health).Others’ collaborations spanned subfactors within a factor area. This was especially notable forHealth. The visualisations suggest that gambling harms research expertise in the UK has considerable room to grow in order to supporta more comprehensive, locally contextualised evidence base for the Framework. To do so, priority harms and funding opportunities will need further consideration. This will require multi-sector and multidisciplinary collaboration consistent with the public health approach underlying the Framework. Future research related to the present analysis will explore the geographic distribution of research activity within the UK, and research collaborations with harms experts internationally.
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Cechinel, Clovis, and Joao Alberto Martins Rodrigues. ASSOCIATION OF DELIRIUM AND FRAGILITY IN HOSPITALIZED ELDERLY: SYSTEMATIC REVIEW. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, September 2021. http://dx.doi.org/10.37766/inplasy2021.9.0022.

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Review question / Objective: What is the relationship between delirium and frailty in hospitalized elderly people? The objective of this research is to analyze the association between frailty and delirium in hospitalized elderly people, through a systematic literature review. Condition being studied: Frailty and delirium in hospitalized aged. Information sources: A specific search strategy for the language of each database was developed using, initially, the Medical Subject Headings (MEsH) descriptor and later translated to specific descriptors (Descriptors in Health Sciences (DeCS) and Embase Subject Headings (Emtree)). The search strategy will be applied by the researchers in the MEDLINE databases through the Pubmed Portal; Scielo; VHL; EMBASE, CINAHL, Scopus and Web of Science through the CAPES Journal Portal; CENTRAL via Cochrane.
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Latzman, Natasha E., Cecilia Casanueva, and Melissa Dolan. Defining and understanding the Scope of Child Sexual Abuse: Challenges and Opportunities. RTI Press, November 2017. http://dx.doi.org/10.3768/rtipress.2017.op.0044.1711.

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The enormous individual, familial, and societal burden of child sexual abuse has underscored the need to address the problem from a public health framework. Much work remains, however, at the first step of this framework — defining and understanding the scope of the problem, or establishing incidence and prevalence estimates. In this occasional paper, we provide an overview of the ways researchers have defined and estimated the scope of child sexual abuse, focusing on agency tabulations and large-scale surveys conducted over the last several decades. More precise estimates of the number of children affected by child sexual abuse would improve the ability of the public health, child welfare, pediatrics, and other communities to prevent and respond to the problem. We recommend using a comprehensive surveillance system to assess and track the scope of child sexual abuse. This system should be grounded by common definitional elements and draw from multiple indicators and sources to estimate the prevalence of a range of sexually abusive experiences.
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